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NCT05013307

Clinical Assessment of Sports Exertion

Enrolling by Invitation
NAAges 10–22InterventionalScreening
Baylor Research Institute
~125 participants
Updated 2026-02-10 on ClinicalTrials.gov
What's tested:CASE

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Heart rate (bpm)
Measured over through study completion, an average of 1.5 hours
+6 more outcomes measured

Conditions

Return to Sport

Explore related trials

Concussion

Where it's being run

1 sites across 1 states
Texas1

Who to contact

This trial hasn't published a contact. View it on ClinicalTrials.gov

Do you actually qualify for this trial?

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Eligibility criteria

Inclusion

10-22 years of age who have participated in organized sport activities within the past 12 months
Diagnosed with a concussion according to international concussion in sport group criteria
Asymptomatic at rest and must be cleared from return-to-play by a qualified healthcare professional no later than 30 days following clearance

Exclusion

Orthopedic or neurologic, or other limitations
History of seizures
Previous or current diagnoses for cardiopulmonary conditions
Medical diagnosis of diabetes and/or currently on medications for diabetes (e.g., insulin)
Uncontrolled asthma
Pregnancy
Currently experiencing symptoms of COVID-19 or \< 7 days since last symptoms
History of moderate or severe traumatic brain injury defined as a brain injury with an associated Glasgow Coma Scale score of 12 or less
Symptom score \>1 point on initial PCSS intake
A current diagnosis of and treatment with medication for attention-deficit/hyperactivity disorder, learning disorder, depression, anxiety, or a history of more than 3 prior concussions
Limited English proficiency
Currently taking prescription medication for concussion related impairments
Anticoagulant or antiplatelet use
History of a medical condition that mimics the signs and symptoms of prolonged concussion symptoms (eg, history of chronic headaches, active migraines, cardiovascular conditions)

What this trial measures

  • Heart rate (bpm)through study completion, an average of 1.5 hours

    Using pulse oximeter placed on index finger heart rate will be recorded.

  • Blood pressure (mmHg)through study completion, an average of 1.5 hours

    Using a manual cuff and auscultation method diastolic and systolic scores will be recorded.

  • Oxygen Saturation (%)through study completion, an average of 1.5 hours

    Using pulse oximeter placed on index finger oxygen saturation will be recorded.

  • Rate of Perceived Exertion (Borg 6-20)through study completion, an average of 1.5 hours

    Using Borg Scale, self report measure of exertion will be recorded. A higher number indicates higher exertion.

  • Self-rated lightheadedness (0-6)through study completion, an average of 1.5 hours

    On a scale of 0-6, a self report measure of lightheadedness will be recorded. A higher number indicates worse lightheadedness.

  • Self-rated dyspnea (Modified Borg 0-10)through study completion, an average of 1.5 hours

    Using Borg scale, self report measure of dyspnea will be recorded. A higher number indicates worse dyspnea.

  • Heart rate reserve (peak-rest), beats/min-1through study completion, an average of 1.5 hours

    Using metabolic cart, heart rate reserve will be recorded via Garmin heart rate strap.